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      Etiology of Maculopapular Rash in Measles and Rubella Suspected Patients from Belarus

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          Abstract

          As a result of successful implementation of the measles/rubella elimination program, the etiology of more and more double negative cases remains elusive. The present study determined the role of different viruses as causative agents in measles or rubella suspected cases in Belarus. A total of 856 sera sent to the WHO National Laboratory between 2009 and 2011 were tested for specific IgM antibodies to measles virus (MV), rubella virus (RV) and human parvovirus B19 (B19V). The negatives were further investigated for antibodies to enterovirus (EV) and adenovirus (AdV). Children of up to 3 years were tested for IgM antibodies to human herpesvirus 6 (HHV6). A viral etiology was identified in 451 (52.7%) cases, with 6.1% of the samples being positive for MV; 2.6% for RV; 26.2% for B19V; 9.7% for EV; 4.6% for AdV; and 3.6% for HHV6. Almost all measles and rubella cases occurred during limited outbreaks in 2011 and nearly all patients were at least 15 years old. B19V, EV and AdV infections were prevalent both in children and adults and were found throughout the 3 years. B19V occurred mainly in 3–10 years old children and 20–29 years old adults. EV infection was most common in children up to 6 years of age and AdV was confirmed mainly in 3–6 years old children. HHV6 infection was mostly detected in 6–11 months old infants. Laboratory investigation of measles/rubella suspected cases also for B19V, EV, AdV and HHV6 allows diagnosing more than half of all cases, thus strengthening rash/fever disease surveillance in Belarus.

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          Spread of Measles Virus D4-Hamburg, Europe, 2008–2011

          The 53 member states of the World Health Organization (WHO) European Region (EUR) have set a goal to eliminate measles and rubella virus transmission by 2015 in Europe ( 1 ). Elimination targets include 95% vaccination coverage with 2 doses of measles virus–containing vaccine (MVCV), an incidence of 11 months). Twenty-six (13%) previously unvaccinated persons had received MVCV after being exposed to measles virus. Three patients had received 2 doses of MVCV. Several of the 216 cases occurred in the Roma ethnic community. Seventy-two cases of measles were reported during the same time in Lower Saxony. Fifty-three cases were clearly related to the outbreak in Hamburg. The first cases in Lower Saxony were reported during week 2 (January) and the last case occurred during week 17 (April) of 2009; the peak of the outbreak occurred during week 14 (April). The connection to the Hamburg outbreak was suggested either by the presence of patients in the emergency department of a Hamburg hospital at the time in question, an epidemiologic link, or the result of the sequencing. Many cases occurred in the Roma ethnic group. Case-patients ranged from 7 months to 42 years of age (median age 15 years); adolescents and younger adults were the main affected age group. Forty-two (79%) case-patients had received no measles vaccination, 10 (19%) had received 1 dose of MVCV, and 1 (2%) had been vaccinated 2 times. In the latter case, primary infection with measles virus was confirmed by PCR and IgM, but IgG was not detected. Five patients received vaccination after exposure, which did not prevent clinical symptoms. Overall, 47 (89%) of measles cases were confirmed by laboratory testing. Eleven (21%) case-patients were admitted to a hospital with complications (e.g., pneumonia, otitis media). Specimens from 12 cases in Hamburg and 18 cases in Lower Saxony were genotyped. All case-patients were infected with the same D4 measles virus variant (MVs/Hamburg.DEU/03.09/[D4], MVs/Harburg.DEU/06.09/[D4], and MVs/Wildeshausen.DEU/21.09/[D4]), none of which were published in the GenBank and MeaNS databases. D4-Hamburg showed 1 mismatch to other D4 measles virus sequences published in GenBank, MVs/Raichur.IND/38.06/[D4]), MVi/Kolar.IND/03.07/1[D4], and MVs/Enfield.GBR/14.07/[D4]; the latter is a strain endemic to the United Kingdom and responsible for the large outbreak there during 2007–2009 (Figure 1). Sequences identical to the Hamburg strain were subsequently identified in London (MVs/London.GBR/5.09/[D4]). Figure 1 Phylogenetic relationships between measles viruses of genotype D4 recently detected in Europe. The measles virus variant D4-Hamburg initiated a long-lasting transmission chain spreading to several European countries during 2008–2011. D4-Hamburg belongs to the D4-Enfield lineage, which is genetically distinct from the previously widespread lineage D4-Bucharest. Phylogenetic analysis is based on a 456-nt sequence encoding the C-terminus of the measles virus nucleocapsid protein. The tree was constructed by the neighbor-joining method by using MacVector version 11.1.2 software (www.macvector.com). Scale bar indicates number of 5-nt deviations per 1,000-nt sequence. GenBank accession numbers are MVi/Montreal.CAN/89 (World Health Organization reference strain; www.cdc.gov/measles/lab-tools/who-table.html), U01976; MVs/Bucharest.ROU/48.04/1, AM849091; MVs/Arad.ROU/38.07/2, HQ704309; MVs/Hamburg.DEU/03.09, HQ436108; MVs/Wildeshausen.DEU/21.09, HQ704360; MVs/Nuernberg.DEU/11.09, HQ436110; MVs/Lodz.POL/27.09, HQ441202; MVs/Belfast.GBR/50.09, GU479875; MVs/Vienna.AUT/13.10/1, HQ704298; MVs/Plovdiv.BGR/23.10/1, HQ436106; MVs/Pyrgos.GRC/19.10, HM802126; MVs/Istanbul.TUR/20.10, HM579947; MVs/Vienna.AUT/24.10, HQ704300; MVs/Kumanovo.MKD/35.10/1, not available (NA); MVs/Lausanne.CHE/02.11, pending; MVs/Plovdiv.BGR/23.10/6, HQ436107; MVs/Ghent.BEL/09.11/1, NA; MVs/Harburg.DEU/06.09, HQ436109; MVs/Wroclaw.POL/13.09, HQ441201; MVs/Silistra.BGR/21.09/1, HQ436104; MVs/Blagoevgrad.BGR/02.10, HQ704345; MVs/Graz.AUT/12.10, HQ441211; MVs/Mannheim.DEU/07.10, HQ704362; MVs/Kerry.IRL/40.09, NA; MVs/Timis.ROU/18.10/1, HQ704313; MVs/Muenchen.DEU/22.10, HQ704350; MVs/Essen.DEU/24.10, HQ704373; MVs/Skopje.MKD/44.10/1, NA; MVs/Karlsruhe.DEU/48.10, pending; MVs/MuenchenDEU/23.10/2, HQ704375; MVs/VelikoTarnovo.BGR/10.11/1, JF754464; MVs/Karlsruhe.DEU/03.09, HQ436113; MVs/London.GBR/5.09, GU120179; MVs/Shumen.BGR/15.09/1, HQ436103; MVs/Pulawy.POL/28.09, HQ441203; MVs/Plovdiv.BGR/03.10/1, HQ436105; MVs/AmaliaDa.GRC/12.10, HM802121; MVs/Eichstaett.DEU/18.10, HQ704346; MVs/Ludwigshafen.DEU/21.10, HQ704349; MVs/Vienna.AUT/23.10, HQ704299; MVs/Belgrad.SRB/24.10, NA; MVs/Neumuenster.DEU/47.10/1, JF754463; MVs/Leskovac.SRB/08.11/1, NA; MVs/Poitiers.FRA/07.09, FN663615; MVs/Manchester.GBR/10.09, GQ370461; MVs/Ravensburg.DEU/17.09, HQ436112; MVs/Offenburg.DEU/18.10, HQ704368; MVs/Ugento.ITA/15.10, HM173092; MVs/Esslingen.DEU/16.10, HQ704364; MVs/Raichur.IND/38.06, EU812270; MVi/Kolar.IND/03.07/1, EU812284; MVs/Enfield.GBR/14.07, EF600554; and MVs/Duesseldorf.DEU/05.09, HQ436111. Transmission to Bulgaria In April 2009, after an absence of 7 years, measles cases began occurring in Bulgaria ( 18 ). Sequencing of 3 specimens from the National Measles Laboratory in Sofia identified MVs/Shumen.BGR/15.09/1-3(D4), identical to D4-Hamburg. The index case-patient in the Bulgaria outbreak was a Roma who worked as a builder in Hamburg and who had visited Razgrad district in northeastern Bulgaria. The outbreak in Bulgaria proceeded from the northeast to the southwest of the country; in 2009, a total of 2,249 cases were reported. A marked increase in case numbers was reported at the end of 2009 and in the beginning of 2010 ( 19 ). From the start of the measles epidemic in April 2009 through the end of week 10 (mid-March) of 2011, a total of 24,379 cases were reported; 24 were fatal ( 20 ). The WHO Regional Reference Laboratory in Berlin received 20 specimens at regular intervals from hospitalized persons. Genotype information was obtained for 19/20 case-patients (Table A1). All viruses detected showed the same sequence (MVs/Shumen.BGR/15.09/1-3[D4], MVs/Silistra.BGR/21.09/1-4[D4], MVs/Blagoevgrad.BGR/02.10[D4], MVs/Plovdiv.BGR/03.10/1-3[D4], MVs/Plovdiv.BGR/23.10/1-5[D4]), and MVs/VelikoTarnovo.BGR/10.11/1-2[D4]), with the exception of MVs/Plovdiv.BGR/23.10/6[D4], characterized by 1 mismatch (Figure 1). Laboratory Investigation of Measles Virus Samples from Bulgaria Measles virus infection was reconfirmed for all 20 case-patients by positive test results for IgM, PCR, or both (Table A1). Results were correlated with the clinical data for each case-patient that had been compiled during hospitalization. For 12 case-patients, vaccination status was unknown; a 7-month-old baby was unvaccinated. Seven case-patients (1, 7, 12, 14, 15, 17, and 18) presented vaccination cards that stated the date of 1 or 2 vaccinations with MVCV (Table A1). All had positive IgM and PCR results; 2 had measles virus–specific IgG (case-patients 7 and 14). IgG avidity testing showed low avidity and thus a vaccination failure for case-patient 7. The equivocal IgM and the mediocre avidity of IgG in patient 14 did not indicate a primary infection. In summary, lack of immunologic response despite documented vaccination was apparent in 6 of 7 case-patients. Transmission of D4-Hamburg Strain in Europe WHO Regional Reference Laboratories in Berlin, Luxembourg, and London receive either specimens or sequence information from the national measles laboratories of 41 European countries. Sequencing of the 450-nt fragment of the N gene showed that the D4-Hamburg strain had further spread in Europe (Figure 2). Samples taken in Poland during the summer of 2009 showed infection with a virus identical to D4-Hamburg (Figure 1); a total of 54 cases were recorded during 2009, the first in June and the last in October. All were linked to 3 outbreaks among Roma residents in the towns of Lodz, Pulawy, and Olpole Lubelskie (MVs/Lodz.POL/27.09[D4], MVs/Pulawy.POL/28.09[D4]) ( 21 ). The virus was also exported to Ireland (MVs/Kerry.IRL/40.09[D4]) from the Roma population and from there into Northern Ireland (MVs/Belfast.GBR/50.09[D4]), with small clusters of associated cases in both countries. Figure 2 Transmission of the D4-Hamburg measles virus strain in Europe, 2008–2011. Arrows mark transmission with known epidemiologic link; ellipsoids mark detection without verified epidemiologic data. IRL, Ireland; GBR, Great Britain; BEL, Belgium; DEU, Germany; POL, Poland; CHE, Switzerland; AUT, Austria; ROU, Romania; SRB, Serbia; BGR, Bulgaria; MKD, Macedonia; GRC, Greece; TUR, Turkey. In Austria, 4 cases classified as D4-Hamburg–associated were detected in March and June 2010. A first sporadic case occurred in Graz in March. A person of Bulgarian nationality who was a member of the Roma ethnic group was infected; he was staying in Austria at the time (MVs/Graz.AUT/12.10[D4]). Three additional cases belonged to a cluster observed among persons in Vienna who spoke Bulgarian (MVs/Vienna.AUT/13.10[D4], MVs/Vienna.AUT/23.10[D4], MVs/Vienna.AUT/24.10[D4]). D4-Hamburg was also seen in Greece, where the first cases and clusters at the beginning of 2010 were identified among families of Roma communities of Bulgarian nationality (MVs/Amaliada.GRC.12.10[D4], MVs/Pyrgos.GRC/19.10[D4]). The virus was then spread to persons of Greek nationality, mainly from Roma communities, reaching 91 laboratory-confirmed measles cases in 2010. Moreover, 2 sporadic cases of D4-Hamburg were observed in 2010 in Romania (MVs/Timis.ROU/18.10/1[D4]). In Turkey, D4-Hamburg was detected in a tourist who stayed in Romania and Bulgaria before visiting Turkey (MVs/Istanbul.TUR/20.10/[D4]). In Serbia, D4-Hamburg was detected in a person with a sporadic case (MVs/Belgrad.SRB/24.10/[D4]) and in the Roma population during an outbreak in Leskovac (MVs/Leskovac.SRB/08.11/1[D4]); 13 persons were infected, of which 3 were hospitalized. The index case-patient was a person who returned at the end of November from Germany (Duisburg). Nearly 400 cases were detected in Macedonia (MVs/Kumanovo.MKD/35.10/1[D4], MVs/Skopje.MKD/44.10/1[D4]). Although we cannot be sure that D4-Hamburg is the only virus contributing to the current outbreaks in Serbia and Macedonia, ongoing transmission of D4-Hamburg is indicated by the recent detection of a sporadic case of D4-Hamburg in Switzerland (MVs/Lausanne.CHE/02.11[D4]; this person probably became infected in Serbia) and by an outbreak of >40 cases in Belgium (MVs/Ghent.BEL/09.11/1[D4]). Reimportation of the D4-Hamburg Strain to Germany In 2010, D4-Hamburg measles virus was reimported to Germany. It appeared first in February in Mannheim, where specimens from 3 case-patients showed a sequence identical to D4-Hamburg (MVs/Mannheim.DEU/07.10[D4]). The virus was introduced by 8 persons from Bulgaria who belonged to a Turkish-speaking minority population, had acquired the infection in Dobrich (Bulgaria), and transmitted the virus to 3 relatives who were living in Mannheim. During June–August 2010, 48 measles cases were reported in Munich; 28 cases occurred among Bulgarian Roma residents in a migrant camp in eastern Munich. Several of these residents worked as cleaning staff at hotels in Munich. From these persons and other hospitalized members of the affected Roma group, the virus spread into the general population. The age of case-patients in Munich ranged from 9 months to 36 years; 7 case-patients were 18 years of age. One case-patient was hospitalized because of encephalitis. Interviews with the help of an interpreter showed that none of the case-patients had MMR vaccination documents. Therefore, vaccination was offered to all inhabitants of the camp. Twenty-eight cases were investigated at the WHO Regional Reference Laboratory in Berlin. Twenty-three cases were associated with MVs/Muenchen.DEU/22.10[D4] identical with D4-Hamburg, and specimens from 5 members of the same group were closely related to MVs/Muenchen.DEU/23.10/2[D4]. Moreover, clusters and sporadic cases of D4-Hamburg were detected in several German cities, e.g., Eichstaett (2 cases, MVs/Eichstaett.DEU/18.10[D4]) and Ludwigshafen (1 case, MVs/Ludwigshafen.DEU/21.10[D4]) in May 2010. These cases were linked to importation of D4-Hamburg from Bulgaria and did not initiate virus spread within Germany. The same virus variant was also detected in a cluster of cases observed in the city of Essen during June–July 2010. This variant was imported from Bulgaria by a citizen of Bulgaria (MVs/Essen.DEU/24.10[D4]) and spread to another citizen of Bulgaria (MVs/Essen.DEU/25.10/1[D4]) and 6 persons of the general population (MVs/Essen.DEU/25.10/2[D4], MVs/Essen.DEU/28.10[D4]). From week 47 (the end of November) on, 8 cases of infection with D4-Hamburg occurred in Neumuenster in northern Germany. This outbreak occurred in a home for migrants mainly from Afghanistan and Serbia (MVs/Neumuenster.DEU/47.10/1[D4]). From week 48 on, 6 cases were seen in another home for migrants in Karlsruhe (MVs/Karlsruhe.DEU/48.10[D4]). Discussion A combination of epidemiologic data and genotyping results enabled us to trace the spread of measles virus D4-Hamburg in Europe. It was imported from London at the end of 2008 to northern Germany (288 cases), then transmitted from Hamburg to Bulgaria, where, after a 7-year absence of measles, an outbreak of 24,379 cases occurred. This was the largest outbreak seen in Europe since an outbreak in the Ukraine in 2006 ( 22 ). Twenty cases from the outbreak in Bulgaria were sampled at different times (April and June 2009, January and June 2010, and March 2011) from persons in distinct districts. The samples were collected initially in northeastern and later in southwestern Bulgaria, thereby following the course of the outbreak. The cases were associated with measles virus sequences such as MVs/Shumen.BGR/15.09[D4], corresponding to D4-Hamburg. The only exception was MVs/Plovdiv.BGR/23.10/6[D4], which showed 1 mismatch but in all probability developed from MVs/Plovdiv.BGR/23.10/1–5[D4]. Because the samples had been obtained at different times and regions, our analysis provides substantial evidence that D4-Hamburg is responsible for the outbreak in Bulgaria, despite the small number of samples. Samples from 6 of 7 persons showed diagnostic markers of a primary measles infection, although these persons had a certificate of prior measles vaccination. Our results therefore demonstrate an urgent need to investigate the vaccination procedures for ethnic minorities. D4-Hamburg was detected subsequently in Poland (54 cases) ( 21 ), Ireland, Northern Ireland, Austria (4 cases), Greece (149 cases) ( 23 ), Serbia (14 cases), Belgium (>40 cases), and Macedonia (>400 cases). Sporadic cases were detected in Romania, Turkey, and Switzerland. More than 70 D4-Hamburg–associated cases were detected in Germany after 8 separate reimportations. Taken together, D4-Hamburg was present in Europe from December 2008 to March 2011—that is, at least 27 full months—and caused >25,300 cases. Because sequencing results are not available quickly in most countries, this transmission chain is probably still ongoing. Circulation of imported measles virus for no longer than 12 months (and therefore endemic transmission according to the WHO definition) is a marker for successful elimination. We suggest, therefore, that the length of a given transmission chain should not be assessed on a national level but at the level of the all 53 countries within the WHO EUR. Epidemiologic data showed that the spread of D4-Hamburg across Europe involved predominantly persons from the Roma ethnic group in Bulgaria. Another transmission chain affecting the Roma population in particular was recorded in 2004 in Romania. An outbreak of >8,000 cases associated with MVs/Bucharest.ROU/48.04[D4] commenced in the Roma population. Subsequent spread of D4-Bucharest by traveling Roma persons was observed until 2007 ( 4 ). The pronounced sequence deviation of D4-Bucharest and D4-Hamburg indicates the presence of at least 2 distinct and successive transmission chains in the Roma population. Both chains were long lasting and associated with a high number of cases, as well as several fatalities. This and other recent outbreaks in Roma communities ( 7 , 24 , 25 ) underline the need for the development of strategies to address this ethnic minority at the regional level and to improve their integration into the respective national health services. The lack of strategies to address reaching the hard-to-reach communities in Europe will clearly have an adverse effect on the measles elimination process. In this context, we want to make clear that elimination of measles virus should not be seen exclusively as a Roma-associated problem. Measles virus is a highly infectious agent and will infect any population with low immunity rates. If itinerant groups are underserved by the national health sector, spread of measles virus is highly probable. Because measles outbreaks in western European countries occur mainly in undervaccinated groups ( 26 ), reaching the hard-to-reach is not the only important challenge. Thus, closing vaccination gaps in a setting of optional vaccination and vaccine skepticism is another important prerequisite that must be met on Europe’s path toward elimination of measles virus.
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            Etiologies of rash and fever illnesses in Campinas, Brazil.

            Few population-based studies of infectious etiologies of fever-rash illnesses have been conducted. This study reports on enhanced febrile-rash illness surveillance in Campinas, Brazil, a setting of low measles and rubella virus transmission. Cases of febrile-rash illnesses in individuals aged <40 years that occurred during the period 1 May 2003-30 May 2004 were reported. Blood samples were collected for laboratory diagnostic confirmation, which included testing for adenovirus, dengue virus, Epstein-Barr virus (EBV), enterovirus, human herpes virus 6 (HHV6), measles virus, parvovirus-B19, Rickettsia rickettsii, rubella virus, and group A streptococci (GAS) infections. Notification rates were compared with the prestudy period. A total of 1248 cases were notified, of which 519 (42%) had laboratory diagnosis. Of these, HHV-6 (312 cases), EBV (66 cases), parvovirus (30 cases), rubella virus (30 cases), and GAS (30 cases) were the most frequent causes of infection. Only 10 rubella cases met the rubella clinical case definition currently in use. Notification rates were higher during the study than in the prestudy period (181 vs 52.3 cases per 100,000 population aged <40 years). Stimulating a passive surveillance system enhanced its sensitivity and resulted in additional rubella cases detected. In settings with rubella elimination goals, rubella testing may be considered for all cases of febrile-rash illness, regardless of suspected clinical diagnosis.
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              Nationwide measles epidemic in Ukraine: the effect of low vaccine effectiveness.

              The WHO European Region has a measles elimination target for 2010. Between September 2005 and mid-June 2006, more than 50,000 measles cases were reported in Ukraine; many reportedly had received two doses of measles vaccine and over 60% were among persons 15-29 years old. To investigate vaccine effectiveness (VE), a case-control study was undertaken in Dnepropetrovsk region. VE for two doses of measles vaccine was 93.1%, providing insufficient population immunity for measles elimination. An additional dose of measles vaccine for these age-cohorts is required if Ukraine is to achieve measles elimination. Other republics of the former Soviet Union also need to consider a supplemental dose of measles vaccine for older age groups identified epidemiologically to be at increased risk for measles even though individuals may have already received two doses.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, USA )
                1932-6203
                2014
                30 October 2014
                : 9
                : 10
                : e111541
                Affiliations
                [1 ]Republican Research and Practical Center for Epidemiology and Microbiology, Minsk, Belarus
                [2 ]Institute of Immunology, Centre de Recherche Public de la Santé/Laboratoire National de Santé, Luxembourg, Luxembourg
                Columbia University, United States of America
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                Conceived and designed the experiments: MY E. Samoilovich CM JH. Performed the experiments: MY GS E. Svirchevskaya. Analyzed the data: MY GS E. Samoilovich E. Svirchevskaya CM JH. Contributed reagents/materials/analysis tools: MY GS E. Samoilovich E. Svirchevskaya CM JH. Wrote the paper: MY E. Samoilovich CM JH.

                Article
                PONE-D-14-01011
                10.1371/journal.pone.0111541
                4214721
                25356680
                24ac3c84-3835-47b6-828c-ac682d01989b
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 8 January 2014
                : 3 October 2014
                Page count
                Pages: 5
                Funding
                The authors wish to thank the Ministry of Cooperation and the Centre de Recherche Public de la Santé in Luxembourg for financial support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Immunology
                Immunity
                Humoral Immunity
                Vaccination and Immunization
                Microbiology
                Virology
                Viral Disease Diagnosis
                Medical Microbiology
                Plant Science
                Plant Pathology
                Infectious Disease Epidemiology
                Medicine and Health Sciences
                Diagnostic Medicine
                Clinical Laboratory Sciences
                Epidemiology
                Infectious Diseases
                Viral Diseases
                Enterovirus Infection
                Erythema Infectiosum
                Exanthem Subitum
                Measles
                Rubella
                Infectious Disease Control
                Public and Occupational Health
                Health Screening

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